scholarly journals Advanced Stage Stuck Gland Adenocarcinoma: Case Report

2020 ◽  
Vol 09 (01) ◽  
pp. 1-7
Author(s):  
Miriam Viviane Baron ◽  
Michele Paula dos Santos ◽  
Gabriela Di Lorenzo Garcia Scherer ◽  
Luis Manuel Ley Dominguez ◽  
Vitória Pereira Itaquy ◽  
...  
Keyword(s):  
2013 ◽  
Vol 5 (1) ◽  
pp. 129-132 ◽  
Author(s):  
P Singh ◽  
S Singh

Background: Sturge-Weber syndrome is a rare congenital neuro- oculo- cutaneous disorder. Objective: To report a very rare unusual case of bilateral manifestation of Sturge Weber syndrome. Case: We report an unusual case of a 17-year-old female with advanced stage of bilateral glaucoma associated with facial nevus extending to the other half of the face as well and bilateral intracranial calcification. Conclusion: Sturge -Weber syndrome can manifest as a bilateral condition. Nepal J Ophthalmol 2013; 5(9):129-132 DOI: http://dx.doi.org/10.3126/nepjoph.v5i1.7841


2019 ◽  
Vol 6 (3) ◽  
pp. 193-198
Author(s):  
Srinivasa Rama Chandra ◽  
◽  
Holley Tyler J ◽  
Ruxandra-Gabriela Coropciuc ◽  
Constantinus Politis ◽  
...  

Author(s):  
Abdul Bari Shaik ◽  
Noor Fathima Shaik

Testicular tumours are a group of heterogenous neoplasms seen commonly in men between the ages of 15 and 35 years. The two main types are seminoma and non-seminomatous germ cell tumour (NSGCT). Testicular cancers are highly treatable and usually curable, even if they present at an advanced stage of the disease with a five-year survival rate of over 95 percent. The symptoms at initial presentation can vary depending on the metastasis, but a nodule or painless swelling of testicle is usually noted. In this case report we will study how a patient with metastatic testicular tumour presents with symptoms indicative of gastrointestinal infection of acute nature with no associated features. We will review current literature on testicular cancers, reasons for delay in treatment and its impact on patient care. 


2014 ◽  
Vol 48 (2) ◽  
pp. 197-202 ◽  
Author(s):  
Andrej Kmetec ◽  
Jera Jeruc

Abstract Background. XP11.2 renal translocation carcinomas are often encountered in paediatric group of patients where they are believed to be rather indolent. They are rare but more aggressive in young adults. They are slow growing, sometimes without characteristic symptoms and their biologic behaviour is uncertain. Case report. We report two cases of this type of tumour in Slovenian young adult males with long and unusual history. Tumours were confirmed imunohistologically by positive reaction for CD10, P504S and TFE3. Conclusions. According to the indications in the literature prognosis of these tumours in young adults depends upon the stage. It seems that cysts, haematomas and necrosis around the kidney are often encountered in these tumours. In advanced stage with lymph nodes involvement or distant metastases, the prognosis is poor. Surgery seems to be basic mode of therapy


2016 ◽  
Vol 9 (2) ◽  
pp. 331-337
Author(s):  
Aki Miyasaka ◽  
Tadaaki Nishikawa ◽  
Eito Kozawa ◽  
Masanori Yasuda ◽  
Keiichi Fujiwara ◽  
...  

Purpose: To describe the postoperative progressive course of advanced-stage adenocarcinoma arising from a mature cystic teratoma (MCT) and review the literature regarding this disease. Methods: A 59-year-old woman visited our hospital with an abdominal mass. Laparotomy showed enlargement of the left ovary and dissemination throughout the abdominal and pelvic cavities. The diagnosis was FIGO stage IIIB adenocarcinoma arising from a MCT. We report this case in detail with a review of the literature. Results: A literature search yielded 9 cases of stage III adenocarcinoma with malignant transformation. Six of these 9 patients died within 12 months after diagnosis. Of the 8 patients who underwent postoperative chemotherapy, 3 survived for over 39 months. The review indicates that prognosis of adenocarcinoma is as poor as that for squamous cell carcinoma arising from a MCT. Conclusions: In general, as with this case, prognosis of advanced adenocarcinoma associated with a MCT is poor. However, we should be aware that not all patients are resistant to chemotherapy.


2003 ◽  
Vol 13 (Suppl 1) ◽  
pp. 56.1-56
Author(s):  
E. Kuscu ◽  
M. Oktem ◽  
S. Erkanli ◽  
A. Haberal ◽  
B. Bilezikci ◽  
...  

2020 ◽  
pp. 112067212094657
Author(s):  
Dario Pasquale Mucciolo ◽  
Vittoria Murro ◽  
Dario Giorgio ◽  
Andrea Sodi ◽  
Ilaria Passerini ◽  
...  

Purpose: To report a case of choroideremia characterized by peripheral retinoschisis with vascular abnormalities and vitreous hemorrhage. Observations: A 58-year-old man affected by advanced-stage choroideremia was diagnosed with peripheral retinoschisis in both eyes. Vitreous hemorrhage was present in the right eye with a peculiar clot-like lesion at the periphery. At the 1-year follow-up, the vitreous hemorrhage had reabsorbed and the vascular clot-like lesion in the periphery had almost completely disappeared. Conclusion and importance: We have reported fundoscopic and OCT features of peripheral-acquired retinoschisis with vascular abnormalities in a patient with choroideremia. OCT examination is extremely useful in clinical evaluation of the peripheral retinal alterations in these cases, where the absence of the retinal pigment epithelium and the choriocapillaris pose many diagnostic difficulties.


Pathology ◽  
2016 ◽  
Vol 48 (6) ◽  
pp. 618-620
Author(s):  
Maximilian Linxweiler ◽  
Bernhard Schick ◽  
Gregor Wolf ◽  
Christian Veith

2009 ◽  
Vol 280 (2) ◽  
pp. 333-335 ◽  
Author(s):  
Orkun Tan ◽  
Edward Luchansky ◽  
Stephen Rosenman ◽  
Tarah Pua ◽  
Masoud Azodi

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